# FDA Inspection 908058 - Mediana USA, Inc. - December 23, 2014

Source: https://www.keypedia.com/records/fda_inspections/mediana-usa-inc/9d05f1e4-e58a-4324-a334-657152be059e
Source feed: FDA_Inspections

> FDA Inspection 908058 for Mediana USA, Inc. on December 23, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 908058
- Company Name: Mediana USA, Inc.
- Inspection Date: 2014-12-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 664940 - 2010-05-28](https://www.keypedia.com/records/fda_inspections/mediana-usa-inc/26935357-90d6-42da-9016-4956f3ef8bf7)
- [FDA Inspection 664940 - 2010-05-28](https://www.keypedia.com/records/fda_inspections/mediana-usa-inc/24508d7e-e4f3-4324-90ff-011a1f618c66)

Company: https://www.keypedia.com/companies/mediana-usa-inc/7d486379-eb4c-4cda-b3cc-535613fae616

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7